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太阳光下正十六烷中多溴二苯醚的光解脱溴途径。

Photolytic debromination pathway of polybrominated diphenyl ethers in hexane by sunlight.

机构信息

School of Public Health, University of Illinois at Chicago, 2121 West Taylor Street, Chicago, IL 60612, USA.

出版信息

Environ Pollut. 2013 Mar;174:194-200. doi: 10.1016/j.envpol.2012.11.035. Epub 2012 Dec 25.

Abstract

The objective of this work is to identify the photolytic debromination pathways of polybrominated diphenyl ethers (PBDEs). Thirteen PBDEs (BDEs 209, 208, 207, 206, 196, 183, 154, 153, 100, 99, 85, 47 and 28) in hexane were individually exposed to sunlight for up to 64 h. A total of 180 PBDEs were screened and 74 BDE debromination products were detected. The disappearance rate constant increased exponentially with increasing number of bromines. While no evident difference in debromination preference among ortho, meta and para bromines was found for heavier congeners, the vulnerability rank order was meta ≥ ortho > para for the lighter congeners (≤8 Br). The total molar mass of PBDEs continuously decreased during sunlight exposure, indicating PBDEs were transformed to non-PBDE compounds. A stochastic least squares debromination pathway model was developed to simulate the reactions and determine the yields to extend the results beyond the experimental observations.

摘要

本工作旨在确定多溴二苯醚(PBDEs)的光解脱溴途径。将十三 种 PBDEs(BDEs 209、208、207、206、196、183、154、153、100、99、85、47 和 28)分别在正己烷中暴露于阳光中,最长达 64 小时。共筛选出 180 种 PBDEs,并检测到 74 种 BDE 脱溴产物。随着溴原子数量的增加,消失速率常数呈指数增长。对于较重的同系物,邻位、间位和对位溴之间没有明显的脱溴偏好差异,但对于较轻的同系物(≤8 Br),易损性顺序为间位≥邻位>对位。在阳光照射期间,PBDEs 的总摩尔质量持续下降,表明 PBDEs 转化为非 PBDE 化合物。开发了随机最小二乘脱溴途径模型来模拟反应并确定产率,以扩展实验观察结果。

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